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Hypophosphatasia: Molecular testing of 19 prenatal cases and discussion about genetic counseling
Brigitte Simon-Bouy*, Agnès Taillandier, Delphine Fauvert, Isabelle Brun-Heath, Jean Louis Serre, Carmen G. Armengod, Martin G. Bialer, Michèle Mathieu, Jacques Cousin, David Chitayat, Jan Liebelt, Barbara Feldman, Marion Gérard-Blanluet, Stefani Körtge-Jung, Cath King, Hannele Laivuori, Martine Le Merrer, Sarju Mehta, Christina Jern, Saba Sharif
*Corresponding author for this work
- Laboratoire SESEP
- Centre Hospitalier de Versailles
- Equipe EA2493
- Université de Versailles Saint-Quentin
- Department of Pediatrics
- Hospital Universitario Río Hortega
- Division of Medical Genetics
- University Hospital
- Service de Cytogénétique
- Amiens University Hospital
- Centre de Génétique
- AP-HP Assistance Publique - Hopitaux de Paris
- Prenatal Diagnosis and Medical Genetics Program (D.C.)
- University Health Network
- Clinical Genetics Service
- Women's and Children's Hospital Adelaide
- Madona Perinatal Service
- Department of Clinical Genetics
- Robert Debré University Hospital
- Prenatal Diagnosis and Genetics
- Department of Clinical Genetics
- Royal United Hospital, Bath
- University of Helsinki
- Département de Genetique
- Université Paris Descartes
- Academic Unit of Medical Genetics and Regional Genetics Service
- St Mary's Hospital London
- University of Gothenburg
- Sahlgrenska University Hospital/Östra
- Service de Génétique Clinique Chromosomique et Moléculaire
- Centre Hospitalier Universitaire de Saint Etienne
- Royal Children's Hospital Brisbane
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(Scopus)